Canonical Allele Identifier: CA1806676555

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102212833C= , CM000670.2:g.102212833C=	GRCh38
NC_000008.10:g.103225061C= , CM000670.1:g.103225061C=	GRCh37
NC_000008.9:g.103294237C=	NCBI36
NG_016617.1:g.31286G= , LRG_788:g.31286G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.846G= MANE Select	NP_056528.2:p.Met282=
ENST00000251810.8:c.846G= MANE Select	ENSP00000251810.3:p.Met282=
NM_001172477.1:c.1062G= , LRG_788t1:c.1062G=	NP_001165948.1:p.Met354=
NM_001172478.1:c.690G=	NP_001165949.1:p.Met230=
NM_001172478.2:c.690G=	NP_001165949.1:p.Met230=
NM_015713.4:c.846G= , LRG_788t2:c.846G=	NP_056528.2:p.Met282=
ENST00000251810.7:c.846G=	ENSP00000251810.3:p.Met282=
ENST00000395910.6:n.233G=
ENST00000395912.6:c.690G=	ENSP00000379248.2:p.Met230=
ENST00000519125.1:n.364G=
ENST00000519317.5:c.210G=	ENSP00000430641.1:p.Met70=
ENST00000519962.5:c.49-4548G=	ENSP00000429140.1:n.49-4548G=
ENST00000522368.5:c.1015G=
ENST00000522394.1:c.179G=	ENSP00000429578.1:n.179G=
ENST00000621845.1:c.684G=	ENSP00000484318.1:p.Met228=